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Spiperone

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Catalog No. T0280Cas No. 749-02-0
Alias Spiropitan, Spiroperidol

Spiperone (Spiropitan) is a spiro butyrophenone analog similar to HALOPERIDOL and other related compounds. It has been recommended in the treatment of SCHIZOPHRENIA.

Spiperone

Spiperone

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Purity: 99.91%
Catalog No. T0280Alias Spiropitan, SpiroperidolCas No. 749-02-0
Spiperone (Spiropitan) is a spiro butyrophenone analog similar to HALOPERIDOL and other related compounds. It has been recommended in the treatment of SCHIZOPHRENIA.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$39In StockIn Stock
10 mg$58In StockIn Stock
25 mg$92In StockIn Stock
50 mgPreferentialIn StockIn Stock
1 mL x 10 mM (in DMSO)$47In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.91%
Color:White
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Product Introduction

Spiperone AI Summary
Spiperone exhibits significant binding affinities and bioactivities across various serotonin and dopamine receptors, as well as other targets. It shows high affinity for the rat 5-hydroxytryptamine 2 receptor (Ki = 1.0 nM) and the dopamine receptor D2 (Ki = 0.045 nM). Additionally, it has moderate to high binding affinity for several other serotonin receptors including 5-HT1A, 5-HT7, and 5-HT2A, with Ki values of 30.0 nM, 19.95 nM, and 1.8 nM, respectively. The compound also exhibits strong inhibitory activity against dopamine D3 and D4 receptors with Ki values of 0.25 nM and 0.33 nM, respectively, and demonstrates potential multi-target activity across dopaminergic and serotonergic systems. Furthermore, Spiperone shows high potency in displacing radioligands from dopamine D2 receptors (IC50 = 0.06 nM) and a significant selectivity towards these receptors compared to others. In terms of adrenergic receptors, it displays notable affinity for the Alpha-1A adrenergic receptor (Ki = 7.2 nM). The compound has demonstrated cardiotoxic effects, such as QTc prolongation in guinea pigs, and exhibits various bioactivities, including inhibition of sodium fluorescein uptake and displacement of [3H]BTX-B from sodium channels. It has also shown antiviral activity, inhibiting SARS-CoV-2 replication in vitro with IC50 values around 20400.0 nM. Overall, the diverse range of bioactivities associated with Spiperone suggests its potential therapeutic applications in neurological disorders, psychiatric conditions, and possibly antiviral treatments, while also highlighting the need for careful consideration of its cardiotoxicity and broad receptor interactions..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Spiperone (Spiropitan) is a spiro butyrophenone analog similar to HALOPERIDOL and other related compounds. It has been recommended in the treatment of SCHIZOPHRENIA.
SynonymsSpiropitan, Spiroperidol
Chemical Properties
Molecular Weight395.47
FormulaC23H26FN3O2
Cas No.749-02-0
SmilesFc1ccc(cc1)C(=O)CCCN1CCC2(CC1)N(CNC2=O)c1ccccc1
Relative Density.1.1714 g/cm3 (Estimated)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 25 mg/mL (63.22 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 4 mg/mL (10.11 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.5286 mL12.6432 mL25.2864 mL126.4318 mL
5 mM0.5057 mL2.5286 mL5.0573 mL25.2864 mL
10 mM0.2529 mL1.2643 mL2.5286 mL12.6432 mL
20 mM0.1264 mL0.6322 mL1.2643 mL6.3216 mL
50 mM0.0506 mL0.2529 mL0.5057 mL2.5286 mL

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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